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Seth M Arum

Showing results (1-10 of 7) with videos related to

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Current Opinion in Endocrinology, Diabetes, and Obesity|October 31, 2008
New developments surrounding the safety of bisphosphonatesSeth M Arum
Journal of Clinical & Translational Endocrinology|October 26, 2017
Management of adynamic bone disease in chronic kidney disease: A brief reviewSwathi K Sista, Seth M Arum
The New England Journal of Medicine|January 24, 2009
Excess iodine from an unexpected sourceSeth M Arum, Xuemei He, Lewis E Braverman
Canadian Respiratory Journal|June 27, 2009
Vitamin D deficiency and chronic lung diseaseChristopher R Gilbert, Seth M Arum, Cecilia M Smith
Endocrine|January 3, 2006
A RET mutation with decreased penetrance in the family of a patient with a "sporadic" pheochromocytomaSeth M Arum, Patricia L M Dahia, Katherine Schneider, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 25, 2022
Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trialDavid Adams, Ivailo L Tournev, Mark S Taylor, et al.
Plos Genetics|August 17, 2005
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomasPatricia L M Dahia, Ken N Ross, Matthew E Wright, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Current Opinion in Endocrinology, Diabetes, and Obesity|October 31, 2008
New developments surrounding the safety of bisphosphonatesSeth M Arum
Journal of Clinical & Translational Endocrinology|October 26, 2017
Management of adynamic bone disease in chronic kidney disease: A brief reviewSwathi K Sista, Seth M Arum
The New England Journal of Medicine|January 24, 2009
Excess iodine from an unexpected sourceSeth M Arum, Xuemei He, Lewis E Braverman
Canadian Respiratory Journal|June 27, 2009
Vitamin D deficiency and chronic lung diseaseChristopher R Gilbert, Seth M Arum, Cecilia M Smith
Endocrine|January 3, 2006
A RET mutation with decreased penetrance in the family of a patient with a "sporadic" pheochromocytomaSeth M Arum, Patricia L M Dahia, Katherine Schneider, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 25, 2022
Efficacy and safety of vutrisiran for patients with hereditary transthyretin-mediated amyloidosis with polyneuropathy: a randomized clinical trialDavid Adams, Ivailo L Tournev, Mark S Taylor, et al.
Plos Genetics|August 17, 2005
A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomasPatricia L M Dahia, Ken N Ross, Matthew E Wright, et al.
Pageof 1